List of variants in gene SLFN14 reported as pathogenic for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001129820.2(SLFN14):c.667C>T (p.Arg223Trp)	rs757188030	0.00001
NM_001129820.2(SLFN14):c.3_4insCTAGTCGACTATA (p.Glu2fs)	rs2072671208
NM_001129820.2(SLFN14):c.652A>G (p.Lys218Glu)	rs869320716
NM_001129820.2(SLFN14):c.657A>T (p.Lys219Asn)	rs869320715
NM_001129820.2(SLFN14):c.659T>A (p.Val220Asp)	rs869320714

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